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Tetrapeptide Inhibitors of the Glutamate Vesicular Transporter (VGLUT)

Quinoline-2,4-dicaboxylic acids (QDCs) bearing lipophilic substituents in the 6- or 7-position were shown to be inhibitors of the glutamate vesicular transporter (VGLUT). Using the arrangement of the QDC lipophilic substituents as a template, libraries of X(1)X(2)EF and X(1)X(2)EW tetrapeptides were...

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Dettagli Bibliografici
Autori principali: Patel, Sarjubhai A., Nagy, Jon O., Bolstad, Erin D., Gerdes, John M., Thompson, Charles M.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2007
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2001293/
https://ncbi.nlm.nih.gov/pubmed/17662605
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmcl.2007.07.006
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